These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
222 related articles for article (PubMed ID: 23874236)
21. Rare deleterious variants in GRHL3 are associated with human spina bifida. Lemay P; De Marco P; Emond A; Spiegelman D; Dionne-Laporte A; Laurent S; Merello E; Accogli A; Rouleau GA; Capra V; Kibar Z Hum Mutat; 2017 Jun; 38(6):716-724. PubMed ID: 28276201 [TBL] [Abstract][Full Text] [Related]
22. Contribution of VANGL2 mutations to isolated neural tube defects. Kibar Z; Salem S; Bosoi CM; Pauwels E; De Marco P; Merello E; Bassuk AG; Capra V; Gros P Clin Genet; 2011 Jul; 80(1):76-82. PubMed ID: 20738329 [TBL] [Abstract][Full Text] [Related]
23. Role of the planar cell polarity gene CELSR1 in neural tube defects and caudal agenesis. Allache R; De Marco P; Merello E; Capra V; Kibar Z Birth Defects Res A Clin Mol Teratol; 2012 Mar; 94(3):176-81. PubMed ID: 22371354 [TBL] [Abstract][Full Text] [Related]
24. Epidemiologic and genetic aspects of spina bifida and other neural tube defects. Au KS; Ashley-Koch A; Northrup H Dev Disabil Res Rev; 2010; 16(1):6-15. PubMed ID: 20419766 [TBL] [Abstract][Full Text] [Related]
25. [Recent perspectives on the development of the central nervous system and the genetic background of neural tube defects]. JoĆ³ JG Orv Hetil; 2009 May; 150(19):873-82. PubMed ID: 19403431 [TBL] [Abstract][Full Text] [Related]
26. The search for genetic determinants of human neural tube defects. Wolujewicz P; Ross ME Curr Opin Pediatr; 2019 Dec; 31(6):739-746. PubMed ID: 31693581 [TBL] [Abstract][Full Text] [Related]
27. Neural tube closure depends on expression of Grainyhead-like 3 in multiple tissues. De Castro SCP; Hirst CS; Savery D; Rolo A; Lickert H; Andersen B; Copp AJ; Greene NDE Dev Biol; 2018 Mar; 435(2):130-137. PubMed ID: 29397878 [TBL] [Abstract][Full Text] [Related]
29. Folate-mediated one-carbon metabolism and neural tube defects: balancing genome synthesis and gene expression. Beaudin AE; Stover PJ Birth Defects Res C Embryo Today; 2007 Sep; 81(3):183-203. PubMed ID: 17963270 [TBL] [Abstract][Full Text] [Related]
30. LRP2 gene variants and their haplotypes strongly influence the risk of developing neural tube defects in the fetus: a family-triad study from South India. K RP; T S; B S; T MK; A J Metab Brain Dis; 2018 Aug; 33(4):1343-1352. PubMed ID: 29728895 [TBL] [Abstract][Full Text] [Related]
31. PAX genes and human neural tube defects: an amino acid substitution in PAX1 in a patient with spina bifida. Hol FA; Geurds MP; Chatkupt S; Shugart YY; Balling R; Schrander-Stumpel CT; Johnson WG; Hamel BC; Mariman EC J Med Genet; 1996 Aug; 33(8):655-60. PubMed ID: 8863157 [TBL] [Abstract][Full Text] [Related]
32. Toward understanding the genetic basis of neural tube defects. Kibar Z; Capra V; Gros P Clin Genet; 2007 Apr; 71(4):295-310. PubMed ID: 17470131 [TBL] [Abstract][Full Text] [Related]
33. High levels of iron supplementation prevents neural tube defects in the Fpn1 Stokes BA; Sabatino JA; Zohn IE Birth Defects Res; 2017 Jan; 109(2):81-91. PubMed ID: 28008752 [TBL] [Abstract][Full Text] [Related]
34. Investigations of single nucleotide polymorphisms in folate pathway genes in Chinese families with neural tube defects. Liu J; Qi J; Yu X; Zhu J; Zhang L; Ning Q; Luo X J Neurol Sci; 2014 Feb; 337(1-2):61-6. PubMed ID: 24326202 [TBL] [Abstract][Full Text] [Related]
35. Heme oxygenase-1 promoter polymorphisms and risk of spina bifida. Fujioka K; Yang W; Wallenstein MB; Zhao H; Wong RJ; Stevenson DK; Shaw GM Birth Defects Res A Clin Mol Teratol; 2015 Sep; 103(9):741-6. PubMed ID: 26173399 [TBL] [Abstract][Full Text] [Related]
36. Mutations in folate transporter genes and risk for human myelomeningocele. Findley TO; Tenpenny JC; O'Byrne MR; Morrison AC; Hixson JE; Northrup H; Au KS Am J Med Genet A; 2017 Nov; 173(11):2973-2984. PubMed ID: 28948692 [TBL] [Abstract][Full Text] [Related]
37. Genetic screening and functional analysis of CASP9 mutations in a Chinese cohort with neural tube defects. Liu XZ; Zhang Q; Jiang Q; Bai BL; Du XJ; Wang F; Wu LH; Lu XL; Bao YH; Li HL; Zhang T CNS Neurosci Ther; 2018 May; 24(5):394-403. PubMed ID: 29365368 [TBL] [Abstract][Full Text] [Related]